114922191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 15720578-G-A

114922191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 15720578-G-T

114922200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720586-G-A

114922200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720586-G-T

114922226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720612-G-A

114922226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720612-G-T

114922256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 15720642-G-A

114922256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 15720642-G-C

114922372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720767-G-A

114922372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720767-G-C

114922372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5 prime UTR variant
orthologous variants: 15720767-G-T

114922423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15720807-G-A

114922423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15720807-G-C

http://identifiers.org/hco/7/GRCh38#114922455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15720837-C-A

114922455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 15720837-C-G

114922455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 15720837-C-T

114922623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 15720948-G-A

114922623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 15720948-G-C

114922623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 15720948-G-T

114922633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 15720959-G-A

114922633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, stop_gained, undefined
orthologous variants: 15720959-G-T

http://identifiers.org/hco/7/GRCh38#114922679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#15720986-C-A

114922679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: intron_variant, undefined
orthologous variants: 15720986-C-T

114922867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15721125-G-A

114922867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15721125-G-C

114922867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15721125-G-T

114922904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15721166-A-G

114922904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15721166-A-T

114922984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15721243-G-A

114922984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15721243-G-T

114923015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 15721252-G-A

114923015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 15721252-G-T

http://identifiers.org/hco/7/GRCh38#114923090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#15721326-C-A

114923090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 15721326-C-G

114923090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 15721326-C-T

114923138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15721377-G-A

114923138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15721377-G-C

114923138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15721377-G-T

114923179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721418-A-G

114923233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721466-C-T

114923243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721477-G-C

114923243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721477-G-T

114923265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721498-G-A

114923265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721498-G-C

114923265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721498-G-T

http://identifiers.org/hco/7/GRCh38#114923350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15721584-C-A

114923350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721584-C-G

114923395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15721622-C-G

114923460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 15721688-T-C

114923463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 15721691-C-G

114923463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 15721691-C-T

114923499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15721742-A-G

114923503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15721746-G-A

114923810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722001-T-A

114923810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722001-T-C

114923961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722131-T-C

114925160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723194-A-G

114925470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723491-T-A

114925532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723554-A-G

114925717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723718-G-T

114925866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723919-G-A

http://identifiers.org/hco/7/GRCh38#114925902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15723955-A-C

114926476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15724487-T-A

114926981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15724972-G-A

114926981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15724972-G-T

114927048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725045-A-G

114927069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725066-G-C

114927069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725066-G-T

114927304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725315-G-A

114927342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725361-A-G

114927342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725361-A-T

114927349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725368-G-A

114927349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725368-G-T

114927410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725428-T-G

114927423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725441-T-A

114927741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725734-C-T

114928170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726206-G-T

114928320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726382-T-A

114928320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726382-T-G

114928339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726400-C-G

114928480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726591-T-A

114928603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726706-T-C

114928858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726808-C-T

http://identifiers.org/hco/7/GRCh38#114929006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15726941-A-C

114929723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727423-C-G

http://identifiers.org/hco/7/GRCh38#114929919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15727589-C-A

114930143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727812-T-C

114930421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728102-A-G

114930444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728125-G-A

114930844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728536-A-G

114931022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728716-T-C

114931067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728755-T-C

114931176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728867-T-C

114931176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728867-T-G

114931183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728874-C-T

114931329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729015-T-C

114931685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729386-A-G

114931706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729411-T-A

114931873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15729644-G-C

114931873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15729644-G-T

114931987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15729845-G-A

114932355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730242-G-A

114932493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730382-G-A

http://identifiers.org/hco/7/GRCh38#114932657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15730509-C-A

114932657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730509-C-T

114932759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730604-G-C

114933136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730947-T-C

114933645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15731258-C-T

114933824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15731430-T-C

114933995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15731616-G-T

114934350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15731949-G-A

114934835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732414-G-A

114935017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732607-A-G

114935074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15732653-G-A

114935203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732766-T-G

114935220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732781-A-G

114935436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732991-A-T

http://identifiers.org/hco/7/GRCh38#114935643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15733148-A-C

114935653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733158-T-C

http://identifiers.org/hco/7/GRCh38#114935888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15733422-A-C

114935929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733465-C-T

114935944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733480-T-C

114936131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733872-A-G

http://identifiers.org/hco/7/GRCh38#114936147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15733888-C-A

114936534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734717-T-C

114936758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734954-T-A

114936805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734999-T-C

http://identifiers.org/hco/7/GRCh38#114936940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15735149-C-A

114937076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735297-G-A

114937614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735821-T-C

114937723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735934-C-T

114937746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735954-G-A

114937916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736099-T-A

114937916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736099-T-C

114938288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736165-G-A

114938339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736217-A-G

114938378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736256-A-G

114938743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736504-C-G

114938757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736518-G-C

114938791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736550-T-A

114938813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736574-G-C

http://identifiers.org/hco/7/GRCh38#114938857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15736625-C-A

114938857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736625-C-T

114938891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736659-T-A

114938919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736687-A-T

114939064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736852-T-C

114939081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736869-T-G

114939120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736903-T-C

114939188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736969-T-A

114939204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736985-T-C

114939283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737062-A-G

114939288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737067-G-A

114939288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737067-G-T

114939523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737306-C-T

114939529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737314-T-C

114940053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737827-G-T

114940081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737855-A-G

114940126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737902-G-A

114940408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738192-C-T

114941307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739881-T-C

114941524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740091-A-G

http://identifiers.org/hco/7/GRCh38#114941869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740443-C-A

http://identifiers.org/hco/7/GRCh38#114941877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740451-C-A

114941877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740451-C-T

114941963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740539-T-G

114942046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740619-G-T

http://identifiers.org/hco/7/GRCh38#114942124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740687-C-A

114942124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740687-C-G

114942124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740687-C-T

http://identifiers.org/hco/7/GRCh38#114942125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740688-C-A

http://identifiers.org/hco/7/GRCh38#114942140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740703-C-A

114942140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740703-C-T

114942143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740706-G-A

114942143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15740706-G-T

http://identifiers.org/hco/7/GRCh38#114942144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15740707-C-A

114942297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 15741009-T-C

http://identifiers.org/hco/7/GRCh38#114942418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15741131-C-A

114942423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741136-A-G

114942434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741147-G-A

114942434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741147-G-C

114942434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741147-G-T

http://identifiers.org/hco/7/GRCh38#114942456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15741167-C-A

114942456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741167-C-G

http://identifiers.org/hco/7/GRCh38#114942480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15741190-C-A

114942480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741190-C-G

114942480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741190-C-T

114942519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741216-T-C

114942756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741435-T-C

114942831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741490-T-A

114942837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741496-G-A

114943033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741691-C-T

114943116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741756-T-C

114943124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741763-C-T

114943154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15741785-C-T

114943697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15742281-T-G

114943698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 15742282-G-T

114943978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15742576-G-A

114944004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15742603-A-G

114944036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15742635-A-G

http://identifiers.org/hco/7/GRCh38#114944039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15742638-C-A

http://identifiers.org/hco/7/GRCh38#114944380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15742968-C-A

http://identifiers.org/hco/7/GRCh38#114944463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15743052-A-C

114944631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15743205-T-C

114944736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15743304-A-G

114944850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15743417-G-A

114945169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15743753-T-C

114945198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15743782-A-G

114945507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744100-A-T

114945514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744107-G-A

114945514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744107-G-T

114945608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744201-G-A

114946741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745425-C-T

114946750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745434-G-A

114946759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745443-G-A

114946760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745444-T-A

114947019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745702-G-A

114947027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745758-C-T

114947140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745869-A-G

114947313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746040-A-G

114947313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746040-A-T

http://identifiers.org/hco/7/GRCh38#114947435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15746163-C-A

114948836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746780-A-G

114948878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746822-G-A

114948929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746868-A-G

114948961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746900-C-T

114948964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746903-T-C

114948977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747138-A-G

114949058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747214-C-T

114949352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747495-G-C

114949759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747891-G-A

114949812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747944-G-C

114950005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748170-A-G

114950085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748244-A-T

http://identifiers.org/hco/7/GRCh38#114950138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15748301-A-C

114950147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748310-A-T

114950207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748367-T-A

114950207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748367-T-C

114950329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748623-G-T

114950344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748638-C-T

http://identifiers.org/hco/7/GRCh38#114950471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15748757-A-C

114950632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748913-T-C

114950722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748997-A-G

114951520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749465-C-T

114951591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749526-A-T

114951640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749573-T-C

114951664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749620-T-A

114951664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749620-T-C

114951840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749790-C-G

114951970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750045-C-G

114952000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750074-C-T

114952214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750297-T-C

114952514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750621-G-C

114952705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750810-T-A

114952705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750810-T-G

114952946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750994-C-T

114953062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751023-C-T

114953174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751125-C-T

114953296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751236-T-C

114953296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751236-T-G

114953321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751258-G-A

114953321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751258-G-C

114953321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751258-G-T

http://identifiers.org/hco/7/GRCh38#114953407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15751342-C-A

114953473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751395-G-A

114953534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751439-G-C

114954096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751640-C-G

114954142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751680-A-T

114954232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751756-T-C

114954811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751852-T-C

http://identifiers.org/hco/7/GRCh38#114954905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15751932-A-C

114955276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752234-C-T

http://identifiers.org/hco/7/GRCh38#114955319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15752264-C-A

114955460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752374-T-C

114955461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752375-A-G

114955502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752416-G-T

114955520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752434-T-C

http://identifiers.org/hco/7/GRCh38#114955572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15752485-C-A

114955572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752485-C-T

114955573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752486-C-T

114955606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752527-T-A

114956680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15753086-G-A

http://identifiers.org/hco/7/GRCh38#114956963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15753357-C-A

114957183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15753567-T-C

114957602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15753974-C-T

114957749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15754123-C-T

114957850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15754221-A-G

114957856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15754227-T-C

114957898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15754273-A-G

http://identifiers.org/hco/7/GRCh38#114958090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15754450-A-C

114958111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15754465-T-A

114958706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755298-G-A

114958721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755308-A-G

114958848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755431-T-C

114958852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755435-C-T

http://identifiers.org/hco/7/GRCh38#114958954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15755516-C-A

114958954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755516-C-T

114959188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755739-G-A

114959325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15755864-A-G

114959587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756254-A-G

114959644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756310-T-C

114959660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756323-A-G

114959733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756387-T-C

114959779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756425-C-T

114959957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756516-A-G

114959980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756539-C-G

114959987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15756546-A-T

114960151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15758359-C-T

http://identifiers.org/hco/7/GRCh38#114960221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15758415-A-C

114962549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15758796-A-G

114962604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15758839-G-T

http://identifiers.org/hco/7/GRCh38#114962731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15758935-C-A

114962785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15758977-T-C

114963038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759219-A-G

114963473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759653-T-A

114963474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759654-G-C

114963479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759659-G-C

114963490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759670-C-T

114963510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15759690-C-T

http://identifiers.org/hco/7/GRCh38#114964052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15759985-C-A

114964884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760414-A-G

114964885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760415-G-A

http://identifiers.org/hco/7/GRCh38#114965074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15760584-C-A

114965074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760584-C-G

114965074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760584-C-T

114965246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760742-T-C

114965268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760754-G-A

114965335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760812-G-C

114965484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15760930-C-T

114965785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761141-T-C

114965797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761154-C-G

114967574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761687-G-A

114967671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761768-T-C

114968129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761899-A-G

114968162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761932-G-C

114968162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15761932-G-T

114968476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15762211-A-T

114968494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15762224-G-A

114968628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15762338-G-A

114968628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15762338-G-T

http://identifiers.org/hco/7/GRCh38#114968677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15762387-C-A

114968728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15762427-G-A

http://identifiers.org/hco/7/GRCh38#114969145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15762845-C-A

http://identifiers.org/hco/7/GRCh38#114969706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15763401-A-C

114969771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15763488-C-G

114969823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15763534-C-T

http://identifiers.org/hco/7/GRCh38#114970515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15764103-C-A

114970582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764165-A-G

114970621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764210-T-C

114970817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764411-G-A

114970908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764443-C-T

114970943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764483-T-G

114970975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764515-C-T

http://identifiers.org/hco/7/GRCh38#114971045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15764578-A-C

114971330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764849-A-G

114971362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15764901-G-T

114971469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765041-G-A

114971507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765083-T-G

114971837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765370-T-C

114971930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765446-G-A

114971977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765500-A-T

114973496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765759-T-C

114973566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765827-T-A

114973724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15765983-T-C

114973763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766033-G-C

114973815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766064-G-A

114973815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766064-G-T

114973884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766132-A-G

114973997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766241-T-C

http://identifiers.org/hco/7/GRCh38#114974057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15766291-C-A

114974057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766291-C-T

114974301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766556-A-G

114974640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15766872-T-C

http://identifiers.org/hco/7/GRCh38#114974691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15766923-C-A

114974787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767020-G-A

114974802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767035-A-G

114974990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767225-A-G

114974991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767226-T-C

114975113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767342-T-A

114975113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767342-T-C

114975136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767365-A-G

114975351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15767583-G-C

114975941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768169-T-C

114975980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768210-C-T

114976208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768441-T-C

114976208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768441-T-G

http://identifiers.org/hco/7/GRCh38#114976348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15768616-C-A

114976349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768617-C-T

114976356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15768624-G-A

114978457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769108-C-G

114978538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769185-G-T

114978579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769228-G-A

114978579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769228-G-T

114978620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769267-G-A

114978837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769441-C-T

114978863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769487-C-T

114978895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769519-G-T

114978937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769539-C-T

114979002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769599-A-G

114979052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769642-G-C

114979076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769667-T-G

114979099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769706-G-C

114979101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769708-G-A

114979202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15769820-A-T

114979362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770024-T-G

114979398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770085-G-A

114979398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770085-G-C

114979398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770085-G-T

114979406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770093-G-T

http://identifiers.org/hco/7/GRCh38#114979416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15770103-C-A

114979419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770106-A-G

http://identifiers.org/hco/7/GRCh38#114979442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15770145-C-A

114979442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770145-C-G

114979459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770162-A-G

114979459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770162-A-T

114979501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 15770208-T-C

114979566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 15770273-T-A

114979566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 15770273-T-C

114979621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 15770331-C-T

114979639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 15770349-C-T

114979657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 15770367-T-A

114979837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770536-G-A

http://identifiers.org/hco/7/GRCh38#114979949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15770614-A-C

114979958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15770623-G-A

http://identifiers.org/hco/7/GRCh38#114980083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15770749-C-A

114980335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15770982-T-C

114980390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15771032-G-A

114980437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15771082-T-C

114980459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15771103-G-A

http://identifiers.org/hco/7/GRCh38#114980607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15771262-C-A

http://identifiers.org/hco/7/GRCh38#114981377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15772056-A-C

114981522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15772170-G-A

114981559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15772207-G-A

114981582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15772225-T-C

http://identifiers.org/hco/7/GRCh38#114981590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15772233-C-A

114981600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15772243-C-T

114981698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15772339-T-C

114984173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15774009-C-T

114984265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15774094-T-C

114984509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15774304-T-A

114984510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15774305-G-A

114984981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15774779-C-T

114985282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775017-T-G

114985325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775059-G-A

114985563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775428-G-T

114985891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775783-T-A

114985917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775809-T-A

114986033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15775914-T-G

114986136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15776009-G-T

114986293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15776164-G-T

114986304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15776174-T-A

114986326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15776225-C-T

114987805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15776901-A-T

114988256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777290-T-C

114988324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777351-G-T

114988422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777524-A-T

114988461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777563-G-T

114988569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777674-T-C

114988661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777759-G-A

114988720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777816-C-G

http://identifiers.org/hco/7/GRCh38#114988764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15777850-C-A

114988793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15777879-G-C

114989080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778145-A-G

114989168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778227-G-A

114989168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778227-G-C

114989187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778247-A-G

114989250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778310-G-C

114989270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778330-G-C

114989460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778533-G-A

http://identifiers.org/hco/7/GRCh38#114989657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15778727-A-C

114989657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778727-A-G

114989681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778751-G-A

114989681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778751-G-T

114989836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778895-G-C

114989863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15778922-C-G

http://identifiers.org/hco/7/GRCh38#114990039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15779154-A-C

114990039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15779154-A-G

http://identifiers.org/hco/7/GRCh38#114990050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15779165-A-C

114990050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15779165-A-G

114990051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15779166-G-A

114990080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15779193-A-G

114998065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783096-G-A

114998129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783139-A-G

114998156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783166-A-G

114998168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783178-A-T

114998169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783179-T-C

114998216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783227-G-A

115000559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15783980-T-G

115000772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15784188-C-T

http://identifiers.org/hco/7/GRCh38#115000933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15784345-A-C

115000940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15784352-C-T

115000982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15784386-G-T

115001006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15784401-G-A

115001323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15784683-C-T

115001673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15785027-G-A

115002273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15785646-C-T

115002284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15785653-G-A

115002386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15785749-C-T

115002981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15786465-G-A

http://identifiers.org/hco/7/GRCh38#115003052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15786536-C-A

115003180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15786671-C-T

115003329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787271-G-A

115003786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787733-C-T

http://identifiers.org/hco/7/GRCh38#115003802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15787749-C-A

115003936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787862-G-A

115003936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787862-G-C

115003949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787875-A-G

115003971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15787892-G-A

115004612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15788097-A-G

115005565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15789757-C-T

115005647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15789841-G-A

115006574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15790753-G-T

115006972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15791366-G-A

http://identifiers.org/hco/7/GRCh38#115007071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15791460-C-A

http://identifiers.org/hco/7/GRCh38#115007104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15791498-C-A

115007362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15791781-G-T

115007489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15791874-A-G

115007492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15791877-A-G

115008154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15792415-A-G

115008586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15792825-G-T

115008731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15792976-C-G

115008731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15792976-C-T

115008793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793036-T-A

115008874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793130-G-A

115008874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793130-G-T

115009097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793307-G-A

115009097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793307-G-T

http://identifiers.org/hco/7/GRCh38#115009117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15793327-C-A

115009134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793346-G-A

115009183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793396-A-G

115009278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793497-G-C

http://identifiers.org/hco/7/GRCh38#115009324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15793543-C-A

115009352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793571-A-G

115009377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793596-A-G

115009652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15793860-G-T

http://identifiers.org/hco/7/GRCh38#115010072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15794279-C-A

115010413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795092-A-G

115010521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795171-G-T

115010667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795345-A-G

115010696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795375-T-A

115010696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795375-T-C

115010769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15795501-C-T

115013348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797241-G-A

115013348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797241-G-T

115013716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797716-C-T

115013811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797812-C-T

115013854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797853-T-G

115013887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797974-G-A

115013898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797985-T-C

115013903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15797990-A-G

115013926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798015-G-T

115013953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798041-C-T

115013959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798047-T-C

115014130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798194-G-T

http://identifiers.org/hco/7/GRCh38#115014144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15798208-A-C

115014144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798208-A-G

115014200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798252-A-G

115014261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798296-T-G

115014369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798382-T-A

115014392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798405-G-A

115014392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798405-G-T

115014395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798408-T-A

115014403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798416-T-G

115014427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798441-C-T

http://identifiers.org/hco/7/GRCh38#115014448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15798465-A-C

115014448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798465-A-G

http://identifiers.org/hco/7/GRCh38#115014635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15798638-C-A

115014635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798638-C-T

http://identifiers.org/hco/7/GRCh38#115014662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15798663-C-A

115014801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15798795-A-G

115015132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799070-T-C

115015145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799083-T-A

115015488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799408-A-G

115015488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799408-A-T

115015566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799505-A-G

115015612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15799539-T-C

http://identifiers.org/hco/7/GRCh38#115016003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15799934-C-A

115016133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800068-C-G

http://identifiers.org/hco/7/GRCh38#115016145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800081-A-C

115016145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800081-A-G

115016153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800089-A-G

http://identifiers.org/hco/7/GRCh38#115016231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800164-C-A

115016233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800166-G-A

115016233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800166-G-T

http://identifiers.org/hco/7/GRCh38#115016859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800411-C-A

http://identifiers.org/hco/7/GRCh38#115016866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800418-A-C

115016866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800418-A-G

115016897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800456-T-C

115016901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800460-G-A

115016915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800474-A-G

115016920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800479-G-A

http://identifiers.org/hco/7/GRCh38#115016989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800538-C-A

115017030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800578-G-A

http://identifiers.org/hco/7/GRCh38#115017056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800592-C-A

http://identifiers.org/hco/7/GRCh38#115017361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15800878-A-C

115017409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800932-G-T

115017426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800955-G-A

115017452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15800993-T-G

115017512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801044-G-A

115017526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801058-G-T

http://identifiers.org/hco/7/GRCh38#115017547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15801080-A-C

115017547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801080-A-G

115017604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801136-T-C

115017824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801340-G-T

115017846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801362-A-G

115017930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801449-G-T

http://identifiers.org/hco/7/GRCh38#115018005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15801526-C-A

115018016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801528-A-G

115018144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801630-C-T

115018236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801695-G-T

115018438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15801883-G-A

115018849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802264-A-G

115018851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802266-G-T

115019021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802520-T-C

115019106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802771-G-T

115019108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802773-T-C

115019109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802774-G-A

115019225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802886-G-A

115019238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802899-A-G

115019295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802960-C-G

115019295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15802960-C-T

http://identifiers.org/hco/7/GRCh38#115019352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#15803069-C-A

115019475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15803188-C-T

115019791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15803458-A-G

115019793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15803460-T-C

115019861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28870
most severe consequence: 3 prime UTR variant
orthologous variants: 15803522-A-G